5. Progressive supranuclear palsy Disease details / Clinical trials / Drug dev / DR info
Clinical trials : 89 / Drugs : 107 - (DrugBank : 40) / Drug target genes : 65 - Drug target pathways : 108
Progressive supranuclear palsy and other diseases between which drug repositioning (DR) might occur (Sakate and Kimura 2021) . Circle size: Number of drugs, Line breadth: Score (Drug repositionability)
| ID | Diseases (Sorted by score) | Score |
|---|---|---|
| 5 | Progressive supranuclear palsy | - |
| 6 | Parkinson disease | 60.082 |
| 13 | Multiple sclerosis/Neuromyelitis optica | 53.116 |
| 2 | Amyotrophic lateral sclerosis | 52.309 |
| 17 | Multiple system atrophy | 41.368 |
| 3 | Spinal muscular atrophy | 37.572 |
| 206 | Fragile X syndrome | 36.011 |
| 8 | Huntington disease | 30.643 |
| 156 | Rett syndrome | 28.720 |
| 22 | Moyamoya disease | 26.436 |
| 70 | Spinal stenosis | 26.138 |
| 18 | Spinocerebellar degeneration | 24.615 |
| 46 | Malignant rheumatoid arthritis | 23.064 |
| 97 | Ulcerative colitis | 22.800 |
| 96 | Crohn disease | 21.066 |
| 21 | Mitochondrial disease | 20.283 |
| 140 | Dorabe syndrome | 20.094 |
| 193 | Prader-Willi syndrome | 19.572 |
| 205 | Fragile X syndrome related disease | 18.726 |
| 34 | Neurofibromatosis | 18.292 |
| 296 | Biliary atresia | 18.162 |
| 144 | Lennox-Gastaut syndrome | 17.465 |
| 158 | Tuberous sclerosis | 16.594 |
| 152 | PCDH19 related syndrome | 16.000 |
| 201 | Angelman syndrome | 15.634 |
| 98 | Eosinophilic gastrointestinal disease | 14.066 |
| 203 | 22q11.2 deletion syndrome | 14.000 |
| 231 | Alpha-1-antitrypsin deficiency | 12.853 |
| 145 | West syndrome | 12.350 |
| 127 | Frontotemporal lobar degeneration | 11.941 |
| 215 | Tetralogy of Fallot | 11.559 |
| 272 | Fibrodysplasia ossificans progressiva | 11.361 |
| 155 | Acquired aphasia with convulsive disorder | 10.593 |
| 298 | Hereditary pancreatitis | 9.405 |
| 169 | Menkes disease | 9.000 |
| 170 | Occipital horn syndrome | 9.000 |
| 36 | Epidermolysis bullosa | 8.802 |
| 113 | Muscular dystrophy | 8.063 |
| 75 | Cushing disease | 7.888 |
| 85 | Idiopathic interstitial pneumonia | 7.351 |
| 102 | Rubinstein-Taybi syndrome | 7.000 |
| 86 | Pulmonary arterial hypertension | 6.580 |
| 84 | Sarcoidosis | 6.292 |
| 118 | Myelomeningocele | 6.219 |
| 4 | Primary lateral sclerosis | 5.992 |
| 26 | HTLV-1-associated myelopathy | 5.305 |
| 256 | Muscle glycogenosis | 5.104 |
| 254 | Porphyria | 4.919 |
| 11 | Myasthenia gravis | 4.825 |
| 233 | Wolfram syndrome | 4.729 |
| 226 | Interstitial cystitis with Hunners ulcer | 4.713 |
| 89 | Lymphangioleiomyomatosis | 4.672 |
| 90 | Retinitis pigmentosa | 4.612 |
| 7 | Corticobasal degeneration | 4.185 |
| 78 | Hypopituitarism | 4.146 |
| 65 | Primary immunodeficiency | 4.102 |
| 299 | Cystic fibrosis | 3.438 |
| 58 | Hypertrophic cardiomyopathy | 3.301 |
| 323 | Aromatic L-amino acid decarboxylase deficiency | 3.000 |
| 57 | Idiopathic dilated cardiomyopathy | 2.949 |
| 280 | Huge arteriovenous malformation with cervicofacial or limb lesion | 2.888 |
| 222 | Primary nephrotic syndrome | 2.390 |
| 288 | Autoimmune acquired coagulation factor deficiency | 2.369 |
| 331 | Idiopathic multicentric castleman disease | 2.164 |
| 210 | Single Ventricle | 2.120 |
| 337 | Homocystinuria | 2.000 |
| 49 | Systemic lupus erythematosus | 1.858 |
| 278 | Huge lymphatic malformation with cervicofacial lesion | 1.855 |
| 212 | Tricuspid atresia | 1.212 |
| 107 | Juvenile idiopathic arthritis | 1.182 |
| 53 | Sjogren syndrome | 1.148 |
| 51 | Scleroderma | 1.141 |
| 149 | Hemiconvulsion hemiplegia epilepsy syndrome | 1.129 |
| 28 | Systemic amyloidosis | 1.049 |
| 251 | Urea cycle disorder | 1.031 |
| 19 | Lysosomal storage disease | 1.027 |
| 111 | Congenital myopathy | 1.000 |